Tuesday, November 18, 2025 1:21:38 PM
Positive Update. Thanks, CUBT Management.
Curative Biotechnology, Inc. Announces Letter to Shareholders
Strategic Update and New Path to Value Creation
Palm Beach Gardens, FL, Nov. 18, 2025 (GLOBE NEWSWIRE) -- Curative Biotechnology Inc. (OTC: CUBT) (“Curative Biotech” or the “Company”), a development-stage biomedical company focused on novel treatments for degenerative eye diseases, today announced the following update to shareholders.
Dear fellow shareholders and interested investors,
We are writing to provide an important update on our business strategy and operational path forward. The Company has been actively pursuing the most efficient and value-accretive route to advance our primary clinical program, the metformin-based eye drops licensed from the National Eye Institute. We are pleased to announce significant changes that we believe will substantially accelerate and de-risk our development path and place us on a sounder financial footing.
These changes include the establishment of a strategic partnership with a key industry player, a revised capital structure, and the official termination of our previous public offering plan.
Key Strategic Developments
1. Strategic Sublicense and Manufacturing Partnership
The Company has decided to seek a manufacturing and/or full product development sublicense agreement for its metformin-based eye drops. We believe this type of relationship will:
Significantly de-risk the operational execution of our trial(s) and ensure a clear, reliable supply chain;
Provide additional non-dilutive funding via upfront and clinical milestone payments;
Accelerate the pathway for future commercialization for intermediate Dry AMD and other degenerative eye diseases.
The Company is in active negotiations with potential partners and believes this process could be completed prior to year end. Of course, there can be no assurance that any of these negotiations will result in a definitive agreement or that any transaction will close.
In addition to pursuing degenerative eye diseases in humans, the Company will focus on similar diseases in canines (K9). Two indications in particular are:
Progressive Retinal Atrophy (PRA), with an estimated prevalence in the U.S. of just under six million dogs;
Central Progressive Retinal Atrophy (CPRA), with an estimated prevalence in the U.S. of under 80,000 diagnoses per year.
CPRA is a K9 disease that closely mimics human Dry AMD and is eligible for the Minor Uses in Major Species accelerated approval pathway, usually requiring a smaller, single 24-dog trial relying heavily on preclinical work to establish reasonable expectation of effectiveness for conditional marketing approval from the FDA Center for Veterinary Medicine (CVM).
We intend to pursue CPRA as the first K9 indication, simultaneously with human Dry AMD, and believe the preclinical data already created for our human trial will provide the evidence of effectiveness required by the CVM. PRA will follow with a single effectiveness trial of roughly 300 dogs.
The veterinary ophthalmic drug market is estimated between $1.5 billion and $2.0 billion annually. Both CPRA and PRA represent unmet medical needs. There is no assurance that the CVM will accept our Dry AMD preclinical research as establishing reasonable expectation of efficacy.
2. Withdrawal of S-1 Registration Statement and Change to Reverse Stock Split Ratio
To better align our capital structure with the Company’s updated strategic direction, the Board has taken two key actions:
Withdrawal of S-1: The Company will formally file to withdraw the previously planned S-1 public offering.
Revised Reverse Stock Split: The Board has approved a revised 150-to-1 reverse split, replacing the prior 400-to-1 requirement.
The reverse split remains subject to FINRA approval, which historically may take weeks to months. There is no assurance of approval or of any impact on the Company’s capital needs.
Path to OTCQB Uplisting
Following execution of the strategic sublicense/manufacturing agreement and completion of the smaller reverse split, the Company intends to submit an application to uplist to the OTCQB Venture Market.
Increased visibility and accessibility to investors, including institutions;
Enhanced transparency and potential improvement in share liquidity;
Positioning for a future uplisting to a national exchange when appropriate.
There is no assurance that the application to uplist will be accepted or that the Company will achieve these objectives.
Conclusion
Our new direction reflects management’s and the Board’s commitment to establishing a more sustainable, de-risked, and strategically aligned future. We believe these actions position Curative Biotech for meaningful advancement of our clinical program and long-term value creation.
Curative Biotechnology, Inc. Announces Letter to Shareholders
Strategic Update and New Path to Value Creation
Palm Beach Gardens, FL, Nov. 18, 2025 (GLOBE NEWSWIRE) -- Curative Biotechnology Inc. (OTC: CUBT) (“Curative Biotech” or the “Company”), a development-stage biomedical company focused on novel treatments for degenerative eye diseases, today announced the following update to shareholders.
Dear fellow shareholders and interested investors,
We are writing to provide an important update on our business strategy and operational path forward. The Company has been actively pursuing the most efficient and value-accretive route to advance our primary clinical program, the metformin-based eye drops licensed from the National Eye Institute. We are pleased to announce significant changes that we believe will substantially accelerate and de-risk our development path and place us on a sounder financial footing.
These changes include the establishment of a strategic partnership with a key industry player, a revised capital structure, and the official termination of our previous public offering plan.
Key Strategic Developments
1. Strategic Sublicense and Manufacturing Partnership
The Company has decided to seek a manufacturing and/or full product development sublicense agreement for its metformin-based eye drops. We believe this type of relationship will:
Significantly de-risk the operational execution of our trial(s) and ensure a clear, reliable supply chain;
Provide additional non-dilutive funding via upfront and clinical milestone payments;
Accelerate the pathway for future commercialization for intermediate Dry AMD and other degenerative eye diseases.
The Company is in active negotiations with potential partners and believes this process could be completed prior to year end. Of course, there can be no assurance that any of these negotiations will result in a definitive agreement or that any transaction will close.
In addition to pursuing degenerative eye diseases in humans, the Company will focus on similar diseases in canines (K9). Two indications in particular are:
Progressive Retinal Atrophy (PRA), with an estimated prevalence in the U.S. of just under six million dogs;
Central Progressive Retinal Atrophy (CPRA), with an estimated prevalence in the U.S. of under 80,000 diagnoses per year.
CPRA is a K9 disease that closely mimics human Dry AMD and is eligible for the Minor Uses in Major Species accelerated approval pathway, usually requiring a smaller, single 24-dog trial relying heavily on preclinical work to establish reasonable expectation of effectiveness for conditional marketing approval from the FDA Center for Veterinary Medicine (CVM).
We intend to pursue CPRA as the first K9 indication, simultaneously with human Dry AMD, and believe the preclinical data already created for our human trial will provide the evidence of effectiveness required by the CVM. PRA will follow with a single effectiveness trial of roughly 300 dogs.
The veterinary ophthalmic drug market is estimated between $1.5 billion and $2.0 billion annually. Both CPRA and PRA represent unmet medical needs. There is no assurance that the CVM will accept our Dry AMD preclinical research as establishing reasonable expectation of efficacy.
2. Withdrawal of S-1 Registration Statement and Change to Reverse Stock Split Ratio
To better align our capital structure with the Company’s updated strategic direction, the Board has taken two key actions:
Withdrawal of S-1: The Company will formally file to withdraw the previously planned S-1 public offering.
Revised Reverse Stock Split: The Board has approved a revised 150-to-1 reverse split, replacing the prior 400-to-1 requirement.
The reverse split remains subject to FINRA approval, which historically may take weeks to months. There is no assurance of approval or of any impact on the Company’s capital needs.
Path to OTCQB Uplisting
Following execution of the strategic sublicense/manufacturing agreement and completion of the smaller reverse split, the Company intends to submit an application to uplist to the OTCQB Venture Market.
Increased visibility and accessibility to investors, including institutions;
Enhanced transparency and potential improvement in share liquidity;
Positioning for a future uplisting to a national exchange when appropriate.
There is no assurance that the application to uplist will be accepted or that the Company will achieve these objectives.
Conclusion
Our new direction reflects management’s and the Board’s commitment to establishing a more sustainable, de-risked, and strategically aligned future. We believe these actions position Curative Biotech for meaningful advancement of our clinical program and long-term value creation.
Bullish
Recent CUBT News
- Curative Biotechnology Engages Sterling Pharmaceutical Services to Manufacture Clinical Supply of Metformin Topical Ophthalmic Therapy • GlobeNewswire Inc. • 04/15/2026 12:08:00 PM
- Curative Biotechnology Announces Reverse Stock Split and Strategic Progress Toward OTCQB Uplisting • GlobeNewswire Inc. • 03/23/2026 11:05:00 PM
- Curative Biotechnology Announces Reverse Stock Split and Strategic Progress Toward OTCQB Uplisting • GlobeNewswire Inc. • 03/23/2026 11:00:00 AM
- Curative Biotechnology Announces Canadian Patent Allowance • GlobeNewswire Inc. • 01/23/2026 01:45:00 PM
- Form RW - Registration Withdrawal Request • Edgar (US Regulatory) • 12/22/2025 06:40:01 PM
- Curative Biotechnology, Inc. Announces Letter to Shareholders • GlobeNewswire Inc. • 11/18/2025 01:15:00 PM
- Form S-1/A - General form for registration of securities under the Securities Act of 1933: [Amend] • Edgar (US Regulatory) • 08/01/2025 08:07:47 PM
- Form SEC STAFF ACTION - SEC Staff Action: ORDER • Edgar (US Regulatory) • 05/09/2025 07:00:02 PM

